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01 1Zhejiang Syncozymes Bio-pharmaceutical Co., Ltd

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ATOGEPANT

NDC Package Code : 84633-1001

Start Marketing Date : 2024-08-21

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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Looking for 1374248-81-3 / Atogepant API manufacturers, exporters & distributors?

Atogepant manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Atogepant API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Atogepant manufacturer or Atogepant supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Atogepant manufacturer or Atogepant supplier.

PharmaCompass also assists you with knowing the Atogepant API Price utilized in the formulation of products. Atogepant API Price is not always fixed or binding as the Atogepant Price is obtained through a variety of data sources. The Atogepant Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Atogepant

Synonyms

Qulipta, Mk-8031, 1374248-81-3, Agn-241689, Atogepant [inn], Atogepant [who-dd]

Cas Number

1374248-81-3

Unique Ingredient Identifier (UNII)

7CRV8RR151

About Atogepant

Atogepant is an oral antagonist of calcitonin gene-related peptide (CGRP) receptors indicated for the prevention of episodic migraine headaches. It was developed by AbbVie and received FDA approval under the brand name Qulipta in September 2021. While its approval was predated by two other members of the same drug family, namely [ubrogepant] and [rimegepant], these agents are indicated only for abortive migraine therapy - atogepant is novel in that it is the first and only oral CGRP antagonist approved for preventative use in migraine. In patients requiring preventative migraine therapy, current practice guidelines recommend the use of certain anti-epileptic medications (e.g. [valproic acid] or [topiramate]) or beta-blockers (e.g. [propranolol]), all of which can be associated with significant adverse effects. The "gepants" family of drugs, including atogepant, are comparatively well-tolerated and may provide a desirable treatment option for patients struggling with adverse reactions to other preventative therapies.

Atogepant Manufacturers

A Atogepant manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atogepant, including repackagers and relabelers. The FDA regulates Atogepant manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atogepant API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Atogepant manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Atogepant Suppliers

A Atogepant supplier is an individual or a company that provides Atogepant active pharmaceutical ingredient (API) or Atogepant finished formulations upon request. The Atogepant suppliers may include Atogepant API manufacturers, exporters, distributors and traders.

click here to find a list of Atogepant suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Atogepant NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Atogepant as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Atogepant API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Atogepant as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Atogepant and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Atogepant NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Atogepant suppliers with NDC on PharmaCompass.

Atogepant Manufacturers | Traders | Suppliers

Atogepant Manufacturers, Traders, Suppliers 1
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We have 1 companies offering Atogepant

Get in contact with the supplier of your choice:

  1. SyncoZymes
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.